# FDA Inspection 1328290 - Kent Laboratories, Inc. - July 28, 2026

Source: https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/5da66d00-e439-4d7b-b81a-a0f8cf448296
Source feed: FDA_Inspections

> FDA Inspection 1328290 for Kent Laboratories, Inc. on July 28, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1328290
- Company Name: Kent Laboratories, Inc.
- Inspection Date: 2026-07-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1328290 - 2026-07-28](https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/136877fa-e88d-47df-b590-753def2d686a)
- [FDA Inspection 994520 - 2016-12-07](https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/2d7909d6-aac4-4877-adba-0021800a6558)
- [FDA Inspection 994520 - 2016-12-07](https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/d2ccd1e8-ab33-47b7-8594-54b1c620c0ec)
- [FDA Inspection 807178 - 2012-11-14](https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/ce20fba5-90fd-4f1f-86c1-a77ab66b4a2f)
- [FDA Inspection 807178 - 2012-11-14](https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/c7369b3e-7f58-4da1-b41f-bc24a5bd178f)

Company: https://www.keypedia.com/companies/kent-laboratories-inc/14a4dc50-b267-4fed-91a9-84490accd72f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7